I haven’t been really keeping up with her as much as I should since holidays were around. I haven’t been raising my light as I should which didn’t do a whole lot. It definitely lightened her up but that also could be from it being in flower. Everything’s been going very good I couldn’t ask for a better grow!!

What a difference a week makes, now starting week 4 and moved them up into their final pots now that I have some space in the tent and they are currently under 600w dual spec and a 315w daylight, I have topped 5 of the 6 but left one as it looks like it’s a stocky plant anyway, they all look like they should be impressive plants so far and visibly growing by the day 😊

Everything was going well during the first week of flowering. I waited until I completed 7 days of flowering to record them. They were flipped on September 20th. The first two days of flowering were difficult because the end of winter reached 35 degrees Celsius inside the tent. Some Bakers showed slight heat stress, the GMOs much less so, and Pure Glitter gave me the impression that she liked high temperatures. I didn't add any additional nutrition other than the flora biostimulant, Tricoderma, and I did a light superficial foliar spray with Bacillus. I'm thinking of maybe adding 0.2g/L of MKP and pure water after four waterings, with an average pH of 6.8 for all solutions. I decided to remove two plants from the tent and flower them outdoors. The goal is to explore their genetics and their development in the sun, even avoiding potential overgrowth. What led me to this decision is that at the beginning of this journey, I had a GMO #4 that only veered for three weeks and had a severe sulfur deficiency. It ended up stalling and I almost killed it. I decided to leave it in the sun with just water, and it simply responded very well. Without adding any type of nutrient, it corrected the deficiency and began flowering. The plant showed many trichomes early and shades of purple in the third week of flowering, which may indicate high anthocyanins. I'm very excited for the flowering of these outdoor and indoor plants. The smell of these girls is already infesting the entire house and even spreading outside. The GMOs I thought were regular, I'm now thinking they might be feminized, as all the seeds I planted have sprouted and are all female. The flower's owner said it's a Mamikos genetic. It's hard to say, but I'm very happy with the smell and development of these plants! I'm very happy with how everything is going, very excited to see the results. See you next week!

Smells like new shoes lol I think I made a decent haul off 315 Watts the buds look frosted and I can’t wait to dry some. I knew what to expect in the coming weeks and if I run this again I think I’ll keep the plants shorter like last time. Highly recommend this Indica strain to anymore looking to make dry ice hash or solvent less! I’ll do the weigh in shortly0

ANTHOCYANIN production is primarily controlled by the Cryptochrome (CR1) Photoreceptor ( !! UV and Blue Spectrums are primary drivers in the production of the pigment that replaces chlorophyll, isn't that awesome! 1. Diverse photoreceptors in plants Many civilizations, including the sun god of ancient Egypt, thought that the blessings of sunlight were the source of life. In fact, the survival of all life, including humans, is supported by the photosynthesis of plants that capture solar energy. Plants that perform photosynthesis have no means of transportation except for some algae. Therefore, it is necessary to monitor various changes in the external environment and respond appropriately to the place to survive. Among various environmental information, light is especially important information for plants that perform photosynthesis. In the process of evolution, plants acquired phytochrome, which mainly receives light in the red light region, and multiple blue light receptors, including his hytropin and phototropin, in order to sense the light environment. .. In addition to these, an ultraviolet light receptor named UVR8 was recently discovered. The latest image of the molecular structure and function of these various plant photoreceptors (Fig. 1), focusing on phytochrome and phototropin. Figure 1 Ultraviolet-visible absorption spectra of phytochrome, cryptochrome, phototropin, and UVR8. The dashed line represents each bioactive absorption spectrum. 2. Phytochrome; red-far red photoreversible molecular switch What is phytochrome? Phytochrome is a photochromic photoreceptor, and has two absorption types, a red light absorption type Pr (absorption maximum wavelength of about 665 nm) and a far-red light absorption type Pfr (730 nm). Reversible light conversion between the two by red light and far-red light, respectively(Fig. 1A, solid line and broken line). In general, Pfr is the active form that causes a physiological response. With some exceptions, phytochrome can be said to function as a photoreversible molecular switch. The background of the discovery is as follows. There are some types of plants that require light for germination (light seed germination). From that study, it was found that germination was induced by red light, the effect was inhibited by subsequent far-red light irradiation, and this could be repeated, and the existence of photoreceptors that reversibly photoconvert was predicted. In 1959, its existence was confirmed by the absorption spectrum measurement of the yellow sprout tissue, and it was named phytochrome. Why does the plant have a sensor to distinguish between such red light and far-red light? There is no big difference between the red and far-red light regions in the open-field spectrum of sunlight, but the proportion of red light is greatly reduced due to the absorption of chloroplasts in the shade of plants. Similar changes in light quality occur in the evening sunlight. Plants perceive this difference in light quality as the ratio of Pr and Pfr, recognize the light environment, and respond to it. Subsequent studies have revealed that it is responsible for various photomorphogenic reactions such as photoperiodic flowering induction, shade repellent, and deyellowing (greening). Furthermore, with the introduction of the model plant Arabidopsis thaliana (At) and the development of molecular biological analysis methods, research has progressed dramatically, and his five types of phytochromes (phyA-E) are present in Arabidopsis thaliana. all right. With the progress of the genome project, Fi’s tochrome-like photoreceptors were found in cyanobacteria, a photosynthetic prokaryotes other than plants. Furthermore, in non-photosynthetic bacteria, a homologue molecule called bacteriophytochrome photoreceptor (BphP) was found in Pseudomonas aeruginosa (Pa) and radiation-resistant bacteria (Deinococcus radiodurans, Dr). Domain structure of phytochrome molecule Phytochrome molecule can be roughly divided into N-terminal side and C-terminal side region. PAS (Per / Arndt / Sim: blue), GAF (cGMP phosphodiesterase / adenylyl cyclase / FhlA: green), PHY (phyto-chrome: purple) 3 in the N-terminal region of plant phytochrome (Fig. 2A) There are two domains and an N-terminal extension region (NTE: dark blue), and phytochromobilin (PΦB), which is one of the ring-opening tetrapyrroles, is thioether-bonded to the system stored in GAF as a chromophore. ing. PAS is a domain involved in the interaction between signal transduction-related proteins, and PHY is a phytochrome-specific domain. There are two PASs and her histidine kinase-related (HKR) domain (red) in the C-terminal region, but the histidine essential for kinase activity is not conserved. 3. Phototropin; photosynthetic efficiency optimized blue light receptor What is phototropin? Charles Darwin, who is famous for his theory of evolution, wrote in his book “The power of move-ment in plants” published in 1882 that plants bend toward blue light. Approximately 100 years later, the protein nph1 (nonphoto-tropic hypocotyl 1) encoded by one of the causative genes of Arabidopsis mutants causing phototropic abnormalities was identified as a blue photoreceptor. Later, another isotype npl1 was found and renamed phototropin 1 (phot1) and 2 (phot2), respectively. In addition to phototropism, phototropin is damaged by chloroplast photolocalization (chloroplasts move through the epidermal cells of the leaves and gather on the cell surface under appropriate light intensity for photosynthesis. As a photoreceptor for reactions such as escaping to the side of cells under dangerous strong light) and stomata (reactions that open stomata to optimize the uptake of carbon dioxide, which is the rate-determining process of photosynthetic reactions). It became clear that it worked. In this way, phototropin can be said to be a blue light receptor responsible for optimizing photosynthetic efficiency. Domain structure and LOV photoreaction of phototropin molecule Phototropin molecule has two photoreceptive domains (LOV1 and LOV2) called LOV (Light-Oxygen-Voltage sensing) on the N-terminal side, and serine / on the C-terminal side. It is a protein kinase that forms threonine kinase (STK) (Fig. 4Aa) and whose activity is regulated by light. LOV is one molecule as a chromophore, he binds FMN (flavin mononucleotide) non-covalently. The LOV forms an α/βfold, and the FMN is located on a β-sheet consisting of five antiparallel β-strands (Fig. 4B). The FMN in the ground state LOV shows the absorption spectrum of a typical oxidized flavin protein with a triplet oscillation structure and an absorption maximum wavelength of 450 nm, and is called D450 (Fig. 1C and Fig. 4E). After being excited to the singlet excited state by blue light, the FMN shifts to the triplet excited state (L660t *) due to intersystem crossing, and then the C4 (Fig. 4C) of the isoaroxazine ring of the FMN is conserved in the vicinity. It forms a transient accretionary prism with the tain (red part in Fig. 4B Eα) (S390I). When this cysteine is replaced with alanine (C / A substitution), the addition reaction does not occur. The effect of adduct formation propagates to the protein moiety, causing kinase activation (S390II). After that, the formed cysteine-flavin adduct spontaneously dissociates and returns to the original D450 (Fig. 4E, dark regression reaction). Phototropin kinase activity control mechanism by LOV2 Why does phototropin have two LOVs? Atphot1 was found as a protein that is rapidly autophosphorylated when irradiated with blue light. The effect of the above C / A substitution on this self-phosphorylation reaction and phototropism was investigated, and LOV2 is the main photomolecular switch in both self-phosphorylation and phototropism. It turns out that it functions as. After that, from experiments using artificial substrates, STK has a constitutive activity, LOV2 functions as an inhibitory domain of this activity, and the inhibition is eliminated by photoreaction, while LOV1 is kinase light. It was shown to modify the photosensitivity of the activation reaction. In addition to this, LOV1 was found to act as a dimerization site from the crystal structure and his SAXS. What kind of molecular mechanism does LOV2 use to photoregulate kinase activity? The following two modules play important roles in this intramolecular signal transduction. Figure 4 (A) Domain structure of LOV photoreceptors. a: Phototropin b: Neochrome c: FKF1 family protein d: Aureochrome (B) Crystal structure of auto barley phot1 LOV2. (C) Structure of FMN isoaroxazine ring. (D) Schematic diagram of the functional domain and module of Arabidopsis thaliana phot1. L, A’α, and Jα represent linker, A’α helix, and Jα helix, respectively. (E) LOV photoreaction. (F) Molecular structure model (mesh) of the LOV2-STK sample (black line) containing A’α of phot2 obtained based on SAXS under dark (top) and under bright (bottom). The yellow, red, and green space-filled models represent the crystal structures of LOV2-Jα, protein kinase A N-lobe, and C-robe, respectively, and black represents FMN. See the text for details. 1) Jα. LOV2 C of oat phot1-to α immediately after the terminus Rix (Jα) is present (Fig. 4D), which interacts with the β-sheet (Fig. 4B) that forms the FMN-bound scaffold of LOV2 in the dark, but unfolds and dissociates from the β-sheet with photoreaction. It was shown by NMR that it does. According to the crystal structure of LOV2-Jα, this Jα is located on the back surface of the β sheet and mainly has a hydrophobic interaction. The formation of S390II causes twisting of the isoaroxazine ring and protonation of N5 (Fig. 4C). As a result, the glutamine side chain present on his Iβ strand (Fig. 4B) in the β-sheet rotates to form a hydrogen bond with this protonated N5. Jα interacts with this his Iβ strand, and these changes are thought to cause the unfold-ing of Jα and dissociation from the β-sheet described above. Experiments such as amino acid substitution of Iβ strands revealed that kinases exhibit constitutive activity when this interaction is eliminated, and that Jα plays an important role in photoactivation of kinases. 2) A’α / Aβ gap. Recently, several results have been reported showing the involvement of amino acids near the A’α helix (Fig. 4D) located upstream of the N-terminal of LOV2 in kinase photoactivation. Therefore, he investigated the role of this A’α and its neighboring amino acids in kinase photoactivation, photoreaction, and Jα structural change for Atphot1. The LOV2-STK polypeptide (Fig. 4D, underlined in black) was used as a photocontrollable kinase for kinase activity analysis. As a result, it was found that the photoactivation of the kinase was abolished when amino acid substitution was introduced into the A’α / Aβ gap between A’α and Aβ of the LOV2 core. Interestingly, he had no effect on the structural changes in Jα examined on the peptide map due to the photoreaction of LOV2 or trypsin degradation. Therefore, the A’α / Aβ gap is considered to play an important role in intramolecular signal transduction after Jα. Structural changes detected by SAXS Structural changes of Jα have been detected by various biophysical methods other than NMR, but structural information on samples including up to STK is reported only by his results to his SAXS. Not. The SAXS measurement of the Atphot2 LOV2-STK polypeptide showed that the radius of inertia increased from 32.4 Å to 34.8 Å, and the molecular model (Fig. 4F) obtained by the ab initio modeling software GASBOR is that of LOV2 and STK. It was shown that the N lobes and C lobes lined up in tandem, and the relative position of LOV2 with respect to STK shifted by about 13 Å under light irradiation. The difference in the molecular model between the two is considered to reflect the structural changes that occur in the Jα and A’α / Aβ gaps mentioned above. Two phototropins with different photosensitivity In the phototropic reaction of Arabidopsis Arabidopsis, Arabidopsis responds to a very wide range of light intensities from 10–4 to 102 μmol photon / sec / m2. At that time, phot1 functions as an optical sensor in a wide range from low light to strong light, while phot2 reacts with light stronger than 1 μmol photon / sec / m2. What is the origin of these differences? As is well known, animal photoreceptors have a high photosensitivity due to the abundance of rhodopsin and the presence of biochemical amplification mechanisms. The exact abundance of phot1 and phot2 in vivo is unknown, but interesting results have been obtained in terms of amplification. The light intensity dependence of the photoactivation of the LOV2-STK polypeptide used in the above kinase analysis was investigated. It was found that phot1 was about 10 times more photosensitive than phot2. On the other hand, when the photochemical reactions of both were examined, it was found that the rate of the dark return reaction of phot1 was about 10 times slower than that of phot2. This result indicates that the longer the lifetime of S390II, which is in the kinase-activated state, the higher the photosensitivity of kinase activation. This correlation was further confirmed by extending the lifespan of her S390II with amino acid substitutions. This alone cannot explain the widespread differences in photosensitivity between phot1 and phot2, but it may explain some of them. Furthermore, it is necessary to investigate in detail protein modifications such as phosphorylation and the effects of phot interacting factors on photosensitivity. Other LOV photoreceptors Among fern plants and green algae, phytochrome ɾphotosensory module (PSM) on the N-terminal side and chimera photoreceptor with full-length phototropin on the C-terminal side, neochrome (Fig. There are types with 4Ab). It has been reported that some neochromes play a role in chloroplast photolocalization as a red light receiver. It is considered that fern plants have such a chimera photoreceptor in order to survive in a habitat such as undergrowth in a jungle where only red light reaches. In addition to this, plants have only one LOV domain, and three proteins involved in the degradation of photomorphogenesis-related proteins, FKF1 (Flavin-binding, Kelch repeat, F-box 1, ZTL (ZEITLUPE)), LKP2 ( There are LOV Kelch Protein2) (Fig. 4Ac) and aureochrome (Fig. 4Ad), which has a bZip domain on the N-terminal side of LOV and functions as a gene transcription factor. 4. Cryptochrome and UVR8 Cryptochrome is one of the blue photoreceptors and forms a superfamily with the DNA photoreceptor photolyase. It has FAD (flavin adenine dinucle-otide) as a chromophore and tetrahydrofolic acid, which is a condensing pigment. The ground state of FAD is considered to be the oxidized type, and the radical type (broken line in Fig. 1B) generated by blue light irradiation is considered to be the signaling state. The radical type also absorbs in the green to orange light region, and may widen the wavelength region of the plant morphogenesis reaction spectrum. Cryptochrome uses blue light to control physiological functions similar to phytochrome. It was identified as a photoreceptor from one of the causative genes of UVR8 Arabidopsis thaliana, and the chromophore is absorbed in the UVB region by a Trp triad consisting of three tryptophans (Fig. 1D). It is involved in the biosynthesis of flavonoids and anthocyanins that function as UV scavengers in plants. Conclusion It is thought that plants have acquired various photoreceptors necessary for their survival during a long evolutionary process. The photoreceptors that cover the existing far-red light to UVB mentioned here are considered to be some of them. More and more diverse photoreceptor genes are conserved in cyanobacteria and marine plankton. By examining these, it is thought that the understanding of plant photoreceptors will be further deepened.

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Time for drying. Btw drying them like this was a bad idea buds are pressed from one side may be conceded to move them, well I still prefer hanging drying 🤪

chopped #1 on 1/21/25 started curing today 1/27/25 chopped #5 on 1/23/25 still hanging and drying. will update with weights and smoke reports and more pictures when dried and cured #1 33 grams. nice big nugs. i really like how the mainline turned out with the final product #5 32 grams smaller buds overall but the yeild is very similar. these are weights after trimming. i did a fairly heavy trim on thesr 2 plants. this diary started with 5 plants but because of my perpetual flowering set up, i have had 3 other diaries for the flowering stages of the other 3. The flowering stage of this diary are only plant #1 and plant #5

seems like i put too much K on this time, guess it was not enough time between because overall temps fell and i didnt take that into consideration. IF your soil temp is lower, then bacteria will slow down taking a longer time to break the minerals down. Going to back off on all feedings for at least a week.

Waiting on a full plant hang dry so will wait at least two weeks maybe three hope ma vegging station holds up n can dae tge damage the now as av said guys this is definitely not the perfect set up am not on good terms with land lord so basically squatting here lol and growing and a got caught with one in this house the land lord doesn’t even know lol 😂

Well I’m pretty excited about this being my first auto grow. These things are really doing awesome I’m pretty impressed I don’t have any experience with them but I feel like they’re all pretty big for their size all of them are really starting to stack up bud. One of the jacks seems to be a few days behind the others in the flowering process. The jacks are both a lot Bashir and flatter the bubblegum and OG a really stretching out nice I love that shape of plant. Soil pH and everything keeps testing good no big issue so far I think one of the plants may have had some small nutrient lockout last week but I flushed it out good. I’ll update this week again soon or maybe not I don’t know thanks for stopping bye be safe ✌️.

What a journey this has been. This girl weighs(dry) 263grams plus 23 grams(untrimmed lower nugs) could have pulled out 350g if let her veg a bit longer. The taste is like sweet candy and soda a hint of citrus. The effects are as follows, creative, giggles and energetic but once its nearly gone out. You will feel really sleepy and when you wake up you will feel really hungry. Anyways, thank you guys who have been following my journey. Next grow will be seeds from Sunkentreasure seeds

Hello! I was absent for most of the grow and unable to properly fill out my journal but my caretaker did a great job following the directions I left. This is my 5x5 tent containing four 5gal sites in a RDWC loop with SE7000 led light. Fed General Hydroponic 10 part @ light strength. Seeds started 2/3 and chopped 4/12. Only training was a topping on week 3 and defoliating after the flower stretch. Not going to lie, I was so hyped to grow this strain that I began growing unimpressed when it seemed the cultivar it shared its space with was outshining them…but I gave the amnesia zkittlez ~2 more weeks and it really turned around. What seemed like just a jungle of loose leaves actually packed on some thick mass and accumulated the most intoxicating aroma of the taste of skittles I didn’t think possible from a plant. Of the 4 plants - 2 are amnesia zkittlez (on the right side in pic). They yielded 816g! 486g of nice buds 103g of trim 330g LARF / lower buds! Total RDWC 5x5 grow was 1429g! It’s only been curing for a couple of weeks but I’m really impressed by the terps and how enjoyable the smoke is! I would definitely recommend and grow again! 👍 Thanks for stopping by!

Oh man, this lavender auto is really starting to come to life! I defoliated it a bit and it didn't even flinch. That's a true sign of a tough plant, and I love it. It's like having a little green warrior in my grow room. And let's talk about Aptus, my nutrient sponsor. I swear by their products, they are the real deal. I've been following their feeding schedule and it's like the plant is just drinking it up. It's like giving a thirsty person a glass of water on a hot day - they just chug it down! Now that we're in the first week of flowering, I'm getting excited to see those buds start to really form. It's like watching a baby grow up right in front of my eyes. And who knows, maybe with all that lavender, the plant will make some moon-inspired magic happen. Hey, I hear there's a blue moon coming up - maybe we'll get some extra magic out of this lavender auto! As always thank you all for stopping by and for supporting me on this journey, i am super passion about growing and fell blessed to have you all with me on this new journey <3 <3 <3 Genetics -Seeds Mafia Lavender Automatic Light - LUMATEK ZEUS 465 COMPACT PRO 
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https://lumatek-lighting.com/ <3 <3 <3 Growers love to you all <3 <3 <3 Auto Lavender Feminized is a very popular type of cannabis, whose strong therapeutic effects are highly appreciated. It has a flowering period of approximately 9-10 weeks and can be grown both indoors and outdoors. It is a resistant variety which can be cared for easily. This variety is mostly appreciated because it produces strong, durable and resistant plants. Its branches and stem usually grow vertically rather than horizontally. It reaches heights of 120 cm and the harvests amount to 90 grams/plant. In addition, it contains high levels of THC- up to 20%. As their name suggests, the plants that grow from Auto Lavender Feminized seeds have a smell and taste similar to those of lavender, also comprising mint and rosemary tones. This is a variety of cannabis that is usually appreciated for its pleasant fragrance and high productivity, seeing as its buds and stem produce an impressive quantity of resin. If you’re looking for another kind of feminized, autoflowering variety, Auto Lavender Feminized will not disappoint you for sure! auto Lavender Feminized is a feminized, autoflowering variety, obtained by crossing the Lavender and Lowryder 2 species. The plants that grow from this variety have a very specific structure: they are tall, vigorous, and have large branches. At the end of the flowering period, the plants acquire an orange-gold shade

I’m starting to see amber trichs on the lower sugar leaves but none on the buds. She can’t be far away now. Next feed will be molasses and then plain water after that. Happy growing.

This week marked the transition into flowering as the light cycle was switched to 12/12, officially initiating bloom 🌸 For the first few days both plants continued normal vegetative growth. The stretch became noticeable after about 3 days, marking the beginning of the flowering phase. • Height approx. ~65 cm • Both plants taller than the Jelly Donutz • Early stretch phase beginning Light intensity was increased to ~750 PPFD ☀️ Clear phenotypic differences continue to develop: • Pheno #2 shows a thicker main stem and stronger vertical growth, with branches staying closer to the main stem • Pheno #1 grows more open and spreads more evenly in all directions Water demand differs slightly between the two: • Pheno #2 watered every 2 days • Pheno #1 watered every 2–3 days 💧 Feeding this week: • 1x BioTabs Bio PK • Otherwise water + BioBizz CalMag Environment remained stable: • 25°C temperature • ~60% RH 🌡️ Very few to no visible white pistils yet, which is normal this early after the flip. The plants are still transitioning hormonally and focusing on stretch before full flower development. Overall a smooth and controlled start into bloom, with stretch beginning and clear structural differences between the phenotypes ?🔥

7. Woche So langsam bekommt Purple Lemonade den Switch für die Bloom, aber sie ist noch etwas hinterher im Vergleich zu den anderen 😁

Die Blätter werden langsam wieder dunkler!